Clinical Research That You Can Depend On

At CliniExperts Research Services, we are focused on conducting high-quality clinical trials in line with ethical and regulatory compliance with the aim to become your go-to Clinical Research Organization (CRO).

About Group

Since 2018, we have been fully dedicated to satisfying this demand by managing complete clinical trials. To this day, we continue to make a mark by providing safe and reliable clinical trial solutions with PAN India coverage.


clinical trials

Expert guidance at each step for your product launch along with hassle free regulatory approvals



Our customized services are designed to address your specific needs and deliver a smooth development pathway for your product launch


Go-to Clinical Research Organization (CRO)

Focusing on high-quality clinical trial management services, we aim to be your one stop CRO

Therapeutic expertise

Leadership team that combines expertise with passion

No. of sites


Investigator Pool


No. of successful studies


Our Team

Leadership team that combines expertise with passion


Dr. Ashwini Kumar

Chief Executive Officer

Dr Ashwini founded CliniExperts in 2009 to actualize his ambitious vision for clinical research in India. His knowledge and leadership skills have resulted in over 5,000 approval for leading pharmaceutical companies.


Rashmi Verma

Chief Operating Officer

Rashmi holds a B.Tech in Computer Science and has considerable experience working in Big Data analytics and software development. Her passion for state-of-the-art technology is complemented by her expertise across project management, strategy execution, and regulatory compliance.


Sushma Srikanth

Vice President, Clinical Operations

Sushma holds a postgraduate degree in Microbiology and a postgraduate diploma in clinical research from Catalyst Clinical Research Services. Her 16 years of research experience with reputed companies in both pharma and CRO have given her the technical edge to efficiently manage all aspects of clinical trials.

Expert Articles

Drug |
Biologicals |
Medical Devices |
Periodic Safety Update Report (PSURs)

Periodic safety update reports (PSUR) are pharmacovigilance documents that allow a periodic but comprehensive assessment of the risk-benefit balance of a medicinal product after it is marketed. The main purpose of the PSUR is to identify new or emerging safety information, as a means of determining changes in the benefit-risk profile of the authorised drug.

Drug |
Medical Devices |
Diagnostic Kits |
Biologicals |
Online submission of SAE reports through SUGAM portal

The New drugs and clinical trials rules, 2019, requires that the investigator, sponsor / CT-NOC holder and ethics committee report all serious adverse events (SAE’s) to the Central Licensing Authority (CLA) within a specified time-frame.

Drug |
Medical Devices |
Diagnostic Kits |
Biologicals |
Consumer Claims |
Conducting Clinical Trial During COVID-19

COVID-19 has caused a massive shift in how we manage clinical trials. Due to inadequate resources and restrictions placed due to the pandemic, companies are struggling to maintain the safety of study participants and staff while ensuring the continuity of ongoing trials.

Drug |
Medical Devices |
Diagnostic Kits |
Biologicals |
Consumer Claims |
Effective Site Management in Clinical Research - Points to Consider

Clinical trials are essential to deliver new therapies and advance medical knowledge and patient care. A key aspect of a successful clinical trial is the efficient management of clinical sites.

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